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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435963Generated: November 3, 2026

Triphenylphosphine → 3-(1-Amino-isoquinolin-6-yloxy)piperidin-1--carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1435963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
Reactant(R)-1-Boc-3-hydroxypiperidineHCID 1514398—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant1-Aminoisoquinolin-6-olHCID 135753991—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product3-(1-Amino-isoquinolin-6-yloxy)piperidin-1--carboxylic acid tert-butyl esterHCID 7756346420.2%

Reaction Steps

To a solution of (R)-3-hydroxypiperidine-1-carboxylic acid tert-butyl ester (209 mg, 1.04 mmol), triphenylphosphine (327 mg, 1.249 mmol), 1-amino-isoquinolin-6-ol (200 mg, 1.249 mmol) in THF (4 ml) and DMF (394 μL) at 0° C., under argon, was added dropwise diethylazodicarboxylate (197 mL) over 5 min. The mixture was then warmed to ambient temperature and stirred for 48 h. Water was then added and the mixture basified with dilute NaOH. The mixture was extracted with ethyl acetate (X3), dried (sodium sulphate) filtered and evaporated under reduced pressure to give a residue. Flash chromatography of the residue on silica (eluent: 2-10% methanol in dichloromethane with 1% aqueous ammonia) gave (S) 3-(1-amino-isoquinolin-6-yloxy)piperidin-1--carboxylic acid tert-butyl ester (72 mg), El-MS: m/z=344.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618985B2
Source datasetuspto-grants-2009_11
ORD IDord-09d2470d721847ecba85d1d9cbd6ed5f
Source noteuspto-grants-2009_11